Canonical Allele Identifier: PA2827432478
Gene: TCF4 HGNC NCBI
ClinVar RCV:
RCV002124646
ClinVar Variation:
1600730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335144.1:p.Pro441Ala
CA402527629
NM_001348215.2:c.1321C>G